A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042429



Internal ID19131648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83407709..83463802hg38UCSC Ensembl
Innerchr14:83874053..83930146hg19UCSC Ensembl
Innerchr14:82943806..82999899hg18UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3856094
hg1956094
hg1856094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532346
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042429
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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